rs200612080
This variant is located in the CPLANE1 gene.
▶GWAS Catalog Trait Associations (1)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (1)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
Hodgkins lymphoma
Osman Y et al. “Functional multigenic variations associated with hodgkin lymphoma.” International Journal of Laboratory Hematology 43(6):1472-1482 (2021)
Allele T
OR —
β 0.030
p 4.0e-12
N 97
Small GWAS
Greater Middle Eastern (Middle Eastern, North African or Persian)
▶ClinVar annotation
Uncertain Significance★★★☆
3 submitters1 publicationAbout CPLANE1
The protein encoded by this gene has putative coiled-coil domains and may be a transmembrane protein. Defects in this gene are a cause of Joubert syndrome (JBTS). [provided by RefSeq, May 2012]
View all CPLANE1 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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